Canonical Allele Identifier: PA102662
Gene: NOG HGNC NCBI

Linked Data

ClinVar Variation Id: 6697
ClinVar RCV Id: RCV000007085 RCV000049267 RCV002512863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005441.1:p.Pro35Arg
CA118431
NM_005450.6:c.104C>G